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rs863225436

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225436(C;C)
Make rs863225436(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position196075339
GeneTFRC
is asnp
is mentioned by
dbSNPrs863225436
ebirs863225436
HLIrs863225436
Exacrs863225436
Varsomers863225436
Maprs863225436
PheGenIrs863225436
hapmaprs863225436
1000 genomesrs863225436
hgdprs863225436
ensemblrs863225436
gopubmedrs863225436
geneviewrs863225436
scholarrs863225436
googlers863225436
pharmgkbrs863225436
gwascentralrs863225436
openSNPrs863225436
23andMers863225436
23andMe allrs863225436
SNP Nexus

SNPshotrs863225436
SNPdbers863225436
MSV3drs863225436
GWAS Ctlgrs863225436
Max Magnitude0
ClinVar
Risk rs863225436(C;C)
Alt rs863225436(C;C)
Reference rs863225436(T;T)
Significance Pathogenic
Disease Combined immunodeficiency Immunodeficiency 46
Variation info
Gene TFRC
CLNDBN Combined immunodeficiency Immunodeficiency 46
Reversed 1
HGVS NC_000003.11:g.195802210A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202386.1, RCV000203305.1,